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4,299,418 works, Canadian by any of four routes.

Every filter state is a URL; the URL is the query; the query is citable via /q/⟨hash⟩. The page, the API and the export parse the same parameters.

The current cohort, streamed from the database: every work column, the machine labels, the provisional scores, and the per-row validation status. Exports are capped at 100,000 rows. Mints a permanent /q/ link for this exact query. The same filters always produce the same link, whoever asks.

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Genetics and Neurodevelopmental Disorders
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Direct Codex and Gemma labels are unvalidated and sparse. Distilled predictions cover the full frame and are also unvalidated. Choose the evidence source explicitly; absence of a direct label is never a negative label.

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The four routes compose: require the funder route and exclude affiliation to get the funder-only stratum no affiliation-based frame ever sees.

1,774 results · 1 filter active ·
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20002025
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Machine labels · sparse coverage
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An unlabeled work is unknown, not a negative. Label coverage is reported on every query.
1,774 works in the cohort · of 4,299,418page 20 of 36

Labels cover 2 of 1,774 works in this cohort. The rest are unlabeled, which is not a negative label: the label table is sparse today and grows as labeling rounds land.

Distilled predictions cover 1,774 of 1,774 works in this cohort. Predictions are machine_predicted_unvalidated. The Gemma side is a direct model label for every work (title-only); the Codex side is a distilled, calibrated classifier. Candidate is the union; consensus is the intersection.

afffundaboutunlabeled
Absence of fragile X syndrome in Nova Scotia
R G BERESFORD
2000· letter· en· Journal of Medical Genetics· Biochemistry, Genetics and Molecular Biology
machine prediction:candidate · noneconsensus · none
10
citations
affunlabeled
SMARCAL1 and replication stress
Carol E. Bansbach, Cornelius F. Boerkoel, David Cortez
2010· article· en· Nucleus· Biochemistry, Genetics and Molecular Biology
machine prediction:candidate · noneconsensus · none
10
citations
aboutno affunlabeled
Adaptive Behavior in Children with Intellectual Disabilities
Hazir Elshani, Eglantina Dervishi, Silva Ibrahımı, Altin Nika, Mimoza Maloku Kuqi
2020· article· en· Mediterranean Journal of Social Sciences· Biochemistry, Genetics and Molecular Biology
machine prediction:candidate · noneconsensus · none
10
citations
affno abstractunlabeled
RAN Translation: Fragile X in the Running
Kaalak Reddy, Christopher E. Pearson
2013· letter· en· Neuron· Biochemistry, Genetics and Molecular Biology
machine prediction:candidate · noneconsensus · none
10
citations
affunlabeled
Rett syndrome: A study of the face
Judith Allanson, Raoul C. M. Hennekam, Ute Moog, Eric Smeets
2011· article· en· American Journal of Medical Genetics Part A· Biochemistry, Genetics and Molecular Biology
machine prediction:candidate · noneconsensus · none
10
citations
fundno affunlabeled
Fragile X syndrome in children
David Acero-Garcés, Wilmar Saldarriaga, Christian Andrés Rojas Cerón, Randi J. Hagerman
2023· review· en· Colombia medica· Biochemistry, Genetics and Molecular Biology
machine prediction:candidate · noneconsensus · none
9
citations
afffundunlabeled
Epigenetics in rare neurological diseases
Chris-Tiann Roberts, Khatereh Saei Arezoumand, Ashraf Kadar Shahib, James Davie, Mojgan Rastegar
2024· review· en· Frontiers in Cell and Developmental Biology· Biochemistry, Genetics and Molecular Biology
machine prediction:candidate · noneconsensus · none
9
citations
fundno affunlabeled
Fragile X Syndrome and Targeted Treatments
Nattaporn Tassanakijpanich, María Jimena Salcedo‐Arellano, Randi J. Hagerman
2020· article· en· Journal of Biomedicine and Translational Research· Biochemistry, Genetics and Molecular Biology
machine prediction:candidate · noneconsensus · none
9
citations

How this was built: Screen · Findings · About